Jump to content

Recommended Posts

Posted

Vaccinations can be as low as 40% effectiveness and as high as 95%. 

In thinking of ways to raise the efficiency of vaccines with < 50% prevention, wouldn't it be more advantageous to use part of a whole cell lysate (taking out the bad stuff)

than using a handful of proteins that produce immunogenicity? At least this way, you're catching all the small interactions with cell components/ proteins that you would miss with just using a

surface protein or flagellin. Sure, you may raise the immune reaction a bit, and produce an elevated fever, but this would be common place in time. If you get a colonoscopy (very short procedure)

you're out of commission for the whole day. 

 

your thoughts?

 

~EE 

Posted

well I'm sure the live or partially dead vaccines are efficient. It's just the vaccines that use a few proteins from the bacteria, like the vaccine for Lyme disease that used DbpA and OspC.

Posted (edited)

Not sure what you are asking. Why in some cases specific antigens are used and in others live/dead vaccines?

Edited by CharonY
Posted

From what I know it's not always possible making an attenuated or inactive version for a vaccine especially for bacteria that has a more complex structure. The chances for side reactions on a subunit vaccine are also lower. When using a subunit vaccine they also use inmunostimulatory agents for a proper inmunogenic reaction.

There's an interesting article I found. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883798/

 

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.